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Items: 2

1.

Developmental delay and seizures with or without movement abnormalities

DEDSM is a neurodevelopmental disorder characterized by global developmental delay, variable intellectual disability, and early-onset seizures with a myoclonic component. Most patients have delayed motor development and show abnormal movements, including ataxia, dystonia, and tremor (summary by Hamdan et al., 2017). [from OMIM]

MedGen UID:
1641343
Concept ID:
C4693376
Disease or Syndrome
2.

Retinitis pigmentosa 59

Any retinitis pigmentosa in which the cause of the disease is a mutation in the DHDDS gene. [from MONDO]

MedGen UID:
462577
Concept ID:
C3151227
Disease or Syndrome

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